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  2. Porphobilinogen deaminase - Wikipedia

    en.wikipedia.org/wiki/Porphobilinogen_deaminase

    Full PBG Deaminase Mechanism. The first step is believed to involve an E1 elimination of ammonia from porphobilinogen, generating a carbocation intermediate (1). [10] This intermediate is then attacked by the dipyrrole cofactor of porphobilinogen deaminase, which after losing a proton yields a trimer covalently bound to the enzyme (2).

  3. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    Elimination reaction of cyclohexanol to cyclohexene with sulfuric acid and heat [1] An elimination reaction is a type of organic reaction in which two substituents are removed from a molecule in either a one- or two-step mechanism. [2] The one-step mechanism is known as the E2 reaction, and the two-step mechanism is known as the E1 reaction ...

  4. E1cB-elimination reaction - Wikipedia

    en.wikipedia.org/wiki/E1cB-elimination_reaction

    An example of the E1cB reaction mechanism in the degradation of a hemiketal under basic conditions. The E1cB elimination reaction is a type of elimination reaction which occurs under basic conditions, where the hydrogen to be removed is relatively acidic, while the leaving group (such as -OH or -OR) is a relatively poor one.

  5. Ohio Unemployment Guide - AOL

    www.aol.com/news/2010-07-12-unemployment-of-ohio...

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  6. Applying for unemployment benefits in Ohio? How long do they ...

    www.aol.com/applying-unemployment-benefits-ohio...

    Applying for unemployment benefits online will help expedite the process. To apply online, visit the Ohio Department of Job and Family Services’ website at un e mployment.ohio.gov and follow the ...

  7. Ohio unemployment claims crash the system - AOL

    www.aol.com/news/2009-01-07-ohio-unemployment...

    According to The Columbus Dispatch, the sudden burst of unemployment claims with the Ohio Department of Job and Family Services has brought the system to its knees. Calls are going unanswered, and ...

  8. Evelyn effect - Wikipedia

    en.wikipedia.org/wiki/Evelyn_effect

    There are two types of elimination reactions, E1 and E2. An E2 reaction is a One step mechanism in which carbon-hydrogen and carbon-halogen bonds break to form a double bond. C=C Pi bond. An E1 reaction is the Ionization of the carbon-halogen bond breaking to give a carbocation intermediate, then the Deprotonation of the carbocation.

  9. Fumarase - Wikipedia

    en.wikipedia.org/wiki/Fumarase

    This led to the conclusion that the formation of S-malate proceeds as E1 elimination - protonation of fumarate to create a carbocation was followed by the addition of a hydroxyl group from H 2 O. However, more recent trials have provided evidence that the mechanism actually takes place through an acid-base catalyzed elimination by means of a ...